Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K010435 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BV Endura with Software Release 2.3- A mobile, diagnostic X-ray image acquisition and viewing system... | 2 | 12/09/2021 | Philips North America Llc |
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